IQVIA is Hiring Clinical Process Associate for Mumbai Location.
Are you skilled in CTA, Clinical Trial Assistant, or Clinical Trial Associate roles? We are looking for individuals with 1-3 years of experience in Clinical Trial Associate positions to join our team. This is a hybrid work opportunity.
Responsibilities:
Assist with clinical trial documentation (e.g., Trial Master File maintenance).
Support data entry, tracking, and verification activities.
Coordinate with clinical team members to gather, review, and manage study documents.
Ensure compliance with GCP (Good Clinical Practice), SOPs, and regulatory requirements.
Participate in audit preparation and quality checks.
Use clinical systems (e.g., CTMS, eTMF) for data management and tracking.
Collaborate cross-functionally with clinical operations, project management, and regulatory teams.
Requirements :
Bachelor’s degree in life sciences, pharmacy, healthcare, or related field.
1–3 years of relevant experience in clinical research or pharmaceutical operations.
Familiarity with clinical trial processes, documentation, and regulatory standards.
Strong attention to detail, organizational, and communication skills.
Proficiency in Microsoft Office and clinical data systems.
Share your updated resume with us at navitha.gouli@iqvia.com.